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FDA food · drug · device recalls, merged

Before you eat it, take it, or plug it in — check.

Big Nope pulls three separate FDA recall feeds into one list per state, so you’re not searching three government databases to get one answer.

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Mendietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 4, 2026

Foods AliveMoringa Leaf Powder

Potential to be contaminated with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 3, 2026

Great ValueOrganic Triple Berry Blend

Possible E. Coli Contamination

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc.Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

LipofitLipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

KofinasGarlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenUndeclaredAnnounced August 31, 2026

Little TemptationsChocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Everything SproutsRobust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

MartinaMangoes

Potential contamination with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)

Recalls nationwide

Data last updated: September 9, 2026 at 1:18 PM UTC

19,424 recalls found
Wording
UnclassifiedRisk not yet known
Medical deviceRecalled May 4, 2026

MEDLINE Medical Procedure Kits labeled as: 1) D AND C PACK, Medline Kit Number/SKU DYNJ53973C; 2) PK CUST CV A&B CABRINI CO, Medline Kit Number/SKU DYNJ60583C.

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98994
Lot/product code:
Medline Product Number/SKU DYNJ53973C: UDI/DI 10195327008864 (each), 40195327008865 (case), Lot Number 21KME435; Medline Product Number/SKU DYNJ53973C: UDI/DI 10195327008864 (each), 40195327008865 (case), Lot Number 21JMC247; Medline Product Number/SKU DYNJ53973C: UDI/DI 10195327008864 (each), 40195327008865 (case), Lot Number 21JMB678; Medline Product Number/SKU DYNJ53973C: UDI/DI 10195327008864 (each), 40195327008865 (case), Lot Number 21IMH919; Medline Product Number/SKU DYNJ60583C: UDI/DI 10195327605582 (each), 40195327605583 (case), Lot Number 24CBO389; Medline Product Number/SKU DYNJ60583C: UDI/DI 10195327605582 (each), 40195327605583 (case), Lot Number 24ABR872.
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 4, 2026

MEDLINE Urethral Catheterization Tray and Bag, Red Rubber Latex, 15 Fr, Medline Product Number/SKU (REF) DYND18350

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98994
Lot/product code:
UDI/DI 10080196996759 (each), 40080196996750 (case); ALL LOTS
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled May 4, 2026

Ice Pop, D'Dioses Fresa Leche, 4 oz (85 g), with UPC 710594511850

May contain not listed on the label milk, pecans, pistachios, yellow #5 and red #40.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1159-2026
Lot/product code:
710594511867,710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362,710594511225
Recalling firm:
D'Dioses Fruit Pops, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled May 4, 2026

Ice Pop, D'Dioses Cookies Cream, 1 Bar (81.7 g), with UPC 710594511362

May contain not listed on the label milk, pecans, pistachios, yellow #5 and red #40.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1167-2026
Lot/product code:
710594511867,710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362,710594511225
Recalling firm:
D'Dioses Fruit Pops, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled May 4, 2026

Ice Pop, D'Dioses Nanche, 1 Bar (81.7 g), with UPC 827912008449

May contain not listed on the label milk, pecans, pistachios, yellow #5 and red #40.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1173-2026
Lot/product code:
710594511867,710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362,710594511225
Recalling firm:
D'Dioses Fruit Pops, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 4, 2026

Pediatric care bed; Product Designation: KayserBett IDA;

If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended, there is an increased risk that the patient (child) or third parties (children) will operate the hand control and trap themselves or others under the bed frame or between the bed frame and the floor. This can lead to serious injuries or even death of the patient (child) or third parties (children).

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98820
Lot/product code:
Product Designation: KayserBett IDA; UDI-DI: 426038961IDAGU; Serial Number: 386, 387, 388, 389, 390, 391, 392, 635, 636, 637, 638, 639, 641, 642, 643, 644, 645, 646, 647, 1072, 1073, 1074, 1075, 1076, 1077, 1078, 1079, 1080, 1081, 1082, 1083, 1085, 1086, 1087, 1088, 1089, 1090, 1110, 1111, 1446, 1447, 1448, 1449, 1648, 1649, 1950, 1975, 1976, 1982, 1983, 1998, 2001, 2003, 2004, 2337, 2338, 2339, 2340, 2341, 2342, 2343, 2344, 2345, 2396, 2763, 2764, 2765, 2766, 2767, 2770, 2771, 2772, 2773, 2774, 3087, 3088, 3089, 3090, 3091, 3092, 3167, 3299, 3300, 3301, 3302, 3303, 3304, 3305, 3306, 3309, 3310, 3311, 3312, 3313, 3314, 3740, 3741, 3760, 4223, 4232, 4233, 4234, 4235, 4236, 4237, 4239, 4240, 4242, 4243, 4244, 4245, 4246, 4247, 4248, 4249, 4250, 4567, 4568, 4569, 4570, 4571, 4572, 4573, 4574, 4575, 4576, 4577, 4578, 4579, 4580, 4581, 4582, 4583, 4584, 4986, 5238, 5254, 5255, 5256, 5257, 5258, 5259, 5637, 5919, 5920, 5921, 5922, 5923, 5924, 5925, 5926, 5937, 5938, 5939, 5940, 5948, 6332, 6338, 6339, 6340, 6341, 6342, 6343, 6344, 6345, 6346, 6347, 6351, 6355, 6795, 6796, 7176, 7177, 7178, 7179, 7180, 7181, 7182, 7183, 7184, 7185, 7186, 7187, 7188, 7189, 7190, 7191, 7192, 7193, 7194, 7195, 7617, 7618, 7619, 7620, 7621, 7622, 7623, 8242, 8243, 8244, 8245, 8588, 8589, 8590, 8591, 8592, 8593, 8594, 8595, 8596, 8597, 8598, 8599, 8600, 8601, 8602, 8603, 8608, 8609, 8691, 8704, 8912, 8921, 8922, 8923, 8924, 8925, 8926, 8927, 8928, 8929, 8930, 9725, 9726, 9727, 10350, 10351, 10352, 10819, 10820, 10821, 10822, 10823, 10824, 10825, 11186, 11367, 11368, 11369, 11370, 11371, 11372, 11797, 11798, 11799, 11800, 11801, 11802, 11803, 11804, 11805, 11806, 11807, 11808, 12247, 12248, 12249, 12250, 12251, 12252, 12253, 12254, 12255, 12256, 12257, 12397, 12398, 12399, 12782, 12783, 12963, 12964, 12965, 12966, 12967, 12968, 12969, 12970, 12971, 12972, 13486, 13487, 13488, 13489, 13490, 13491, 13492, 13493, 13494, 13495, 13496, 13497, 13912, 13913, 13914, 13915, 13916, 13917, 13918, 14942, 14944, 14952, 14953, 15912, 15913, 15914, 16403, 16404, 16405, 16406, 16407, 16408, 16409, 16410, 16411, 16984, 16985, 16986, 16987, 16988, 16989, 16990, 16991, 16992, 16993, 16994, 17577, 17578, 17579, 17580, 17581, 17582, 17583, 17584, 17585, 17586, 17587, 18494, 19112, 19113, 19114, 20151, 20152, 20153, 20154, 20155, 20156, 20157, 20158, 20963, 20964, 20965, 20966, 20967, 20968, 20969, 20970, 20972, 21192, 21193, 21194;
Recalling firm:
KAYSERBETTEN GMBH & CO. KG
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled May 4, 2026

Ice Pop, D'Dioses Limon, 4 oz (85 g), with UPC 710594511836

May contain not listed on the label milk, pecans, pistachios, yellow #5 and red #40.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1169-2026
Lot/product code:
710594511867,710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362,710594511225
Recalling firm:
D'Dioses Fruit Pops, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 4, 2026

MEDLINE Urethral Catheterization Tray, Red Rubber Latex, Medline Product Number/SKU (REF), French sizes: 1. DYNC1816, 15 Fr; 2. DYND10350, 15 Fr.

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98994
Lot/product code:
1. DYNC1816, UDI/DI 10080196990627 (each), 40080196990628 (case); 2. DYND10350, UDI/DI 10080196028665 (each), 40080196028666 (case). ALL LOTS
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled May 4, 2026

Ice Pop, D'Dioses Mango, 3.7 oz (81.7 g), with UPC 827912008494

May contain not listed on the label milk, pecans, pistachios, yellow #5 and red #40.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1171-2026
Lot/product code:
710594511867,710594511850, 710594511560, 827912008456, 8279120084732, 710594511829, 71059511812, 827912008487, 827912008548, 710594511836, 827912008531, 827912008494, 827912008593, 827912008449, 710594511362,710594511225
Recalling firm:
D'Dioses Fruit Pops, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

#007415 Fiery Hot, Net Wt: 25 lbs. JCB Flavors, 1224 Clark Street, Watertown, WI 53094.

Products may be potentially contaminated with Salmonella.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0883-2026
Lot/product code:
Lot: 088393-1-1
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

#003740 Dill & Garlic Seasoning, Net Wt: 10 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094.

Products may be potentially contaminated with Salmonella.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0888-2026
Lot/product code:
Lot# 087307-1-1
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled May 1, 2026

Primidone Tablets, USP, 50 mg, 100 Tablets (10 x 10 unit dose blister) per carton, Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC: 68084-202-01; Individual Dose NDC: 68084-202-11

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0537-2026
Lot/product code:
Lot 1028739, exp 12/31/2027; Lot 1025622, exp 06/30/2027
Recalling firm:
Amerisource Health Services LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2026

DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.

System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.

Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98940
Lot/product code:
Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.
Recalling firm:
Philips North America Llc
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled May 1, 2026

Primidone Tablets, USP, 250 mg, 100 Tablets (10 x 10 unit dose blister) per carton, Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC: 68084-203-01; Individual Dose NDC: 68084-203-11

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0536-2026
Lot/product code:
Lot#: 1027583, Exp 09/30/2027
Recalling firm:
Amerisource Health Services LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

Popping Topping, Sour Cream & Onion Flavored Popcorn Seasoning, Net Wt: 1.6oz. UPC 0 31851-01001 6. Distributed By: Butler's Pantry, 1224 Clark St. Watertown, WI 53094.

Products may be potentially contaminated with Salmonella.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0886-2026
Lot/product code:
Lot: 057596
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

#800414/003729Butter Parsley, Net Wt: 50 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094

Products may be potentially contaminated with Salmonella.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0885-2026
Lot/product code:
Lot: 087735-1-1
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

#007560 Fiery Hot Seasoning (Reduced Salt), Net Wt: 25 lbs. JCB Flavors, 1224 Clark Street, Watertown, WI 53094

Products may be potentially contaminated with Salmonella.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0881-2026
Lot/product code:
Lot: 087861-1-1
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

#0083004 Ranch Seasoning, Net Wt: 25 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094.

Products may be potentially contaminated with Salmonella.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0889-2026
Lot/product code:
Lot# 087002-2-1
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2026

Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1, a combination of an infant incubator and an infant warmer, Model Numbers 2082844-001-XXX

GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98986
Lot/product code:
UDI-DI: 010084068211686221; Serial Numbers: TAB24430068SA TAB24430069SA TAB24430070SA TAB24430071SA TAB26011006SA TAB26011009SA TAB26021001SA TAB26061022SA TABW63370 TAB24300033SA TABV60214 TABW63378 TAB24240010SA TABV62327 TABA70043 TABA70053 TABA70054 TABA70055 TABZ72515 TABV60081 TABV60219 TABV60221 TABV60223 TABV60224 TAB25351023SA TAB25501502SA TAB25501503SA TAB25501530SA TAB25501531SA TAB26021501SA TAB26021503SA TAB26101502SA TAB26101503SA TAB26101507SA TAB26101509SA TAB26101510SA TAB26101511SA TAB26101512SA TAB26101513SA TAB26101515SA TAB26101516SA TAB26101517SA TAB26101519SA TAB26101520SA TAB26101521SA TABX63854 TABX63855 TABX63856 TAB25111019SA TAB24160010SA TABY70926 TABY70987 TABX63393 TAB24280002SA TABV60007 TABV60203 TABW63326 TABX62677 TABX62757 TABX63717 TABX63718 TABY71177 TAB24180045SA TAB24180046SA TAB24180047SA TAB24280001SA TAB25081073SA TAB25081074SA TABB70452 TABB70464 TABB70550 TABB70572 TABX63665 TABX63769 TABX63776 TAB24330009SA TAB24330010SA TAB24330011SA TAB24330012SA TAB24330013SA TAB24330014SA TAB24330015SA TAB24330016SA TAB24330017SA TAB24330018SA TAB24330021SA TAB24430028SA TAB25101068SA TAB25101069SA TAB25101070SA TAB25101071SA TAB25101072SA TAB25101073SA TAB25101074SA TAB25101075SA TAB25101076SA TAB25101077SA TAB25101078SA TAB25101079SA TAB25101080SA TAB25101081SA TAB25101082SA TAB25101083SA TAB25111000SA TAB25111001SA TAB25111002SA TAB25111003SA TAB25111004SA TAB25111009SA TAB25111010SA TAB25111011SA TAB25111012SA TAB25111013SA TAB25421013SA TAB25421014SA TAB25421015SA TAB25421016SA TABX62269 TABZ70640 TAB26061051SA TAB26071039SA TAB26081028SA TAB26081035SA TAB26081042SA TABW62610 TABW62689 TABW62731 TABX62268 TABX63359 TABX63374 TABX63603 TABX63614 TABX63616 TABA71644 TABA71768 TABW63180 TABZ70669 TAB24500004SA TAB24500005SA TAB24500006SA TAB24500007SA TAB25121048SA TABV61088 TABV61128 TABV61129 TABV61130 TABV61295 TABV61301 TABV61306 TABV61313 TABV61326 TABV61333 TABV61335 TABV61336 TABV61338 TABV61350 TABV61352 TABV61355 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TABB70847 TABB71365 TABB71501 TABB71514 TABB71548 TABB71550 TABB71551 TABB71573 TABB71574 TABB71575 TABB71576 TABB71611 TABB71614 TABB71617 TABB71618 TABB71620 TAB23410042SA TAB23450037SA TAB23470001SA TAB23470007SA TAB23480027SA TAB23480028SA TAB23480030SA TAB23480035SA TAB23480037SA TAB23480038SA TAB23480039SA TAB23480040SA TAB22340001SA TAB24060005SA TAB24420088SA TAB24430012SA TAB24430013SA TAB24430014SA TAB24430016SA TAB24430017SA TAB24430018SA TAB24430019SA TAB24430020SA TAB24430021SA TAB24430022SA TAB24430023SA TAB24430024SA TAB24430025SA TAB24430026SA TAB24430027SA TAB24440001SA TAB24440003SA TAB24440004SA TAB24440005SA TAB24440006SA TAB24440007SA TAB24440008SA TAB24440010SA TAB24440011SA TAB24440012SA TAB24440013SA TAB24440014SA TAB24440015SA TAB24440016SA TABA70297 TAB24430034SA TAB24370093SA TAB24370099SA TAB24370101SA TAB24370102SA TAB24370103SA TAB24370104SA TAB24370105SA TAB24370106SA TAB24370107SA TAB24370108SA TAB24370109SA TAB24370110SA TAB24370111SA TAB24370112SA 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TAB24380111SA TAB244… (truncated, 269577 characters total — see the official FDA record for the full value)
Recalling firm:
GE Medical Systems, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2026

CGuard Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98922
Lot/product code:
UDI: 07290120281783; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026
Recalling firm:
INSPIREMD Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2026

CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98922
Lot/product code:
UDI: 07290120281776; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026
Recalling firm:
INSPIREMD Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2026

CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98922
Lot/product code:
UDI: 07290120281738; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026
Recalling firm:
INSPIREMD Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

White Cheddar Seasoning packaged in the following sized containers: 1. Net Wt. 1.2 oz (34g) Distributed by: Fireworks Popcorn, Division of Jonco Industries, Milwaukee, WI 53218. Sold in a Fireworks Popcorn Popping & Toppings gift set. 2. Net Wt. 1.6 oz. (45g) UPC 7 36659-26501 8. Distributed by: Fireworks Popcorn, Division of Jonco Industries, Milwaukee, WI 53218. Sold at West Allis Cheese and Sausage retail store. 3. Net Wt 0.7 oz (19g) Williams Sonoma, Not for Retail Sale. Sold in a Williams Sonoma branded Popcorn Sampler Gift Box.

Products may be potentially contaminated with Salmonella.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0890-2026
Lot/product code:
1. Lot# 088594-5-1 2. Lot# 088594-7-1 3. Lot# 088594-2-1
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 1, 2026

#003020 Sour Cream & Onion, Net Wt: 10 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094.

Products may be potentially contaminated with Salmonella.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0887-2026
Lot/product code:
Lot# 087307-2-1
Recalling firm:
JCB Flavors, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 1, 2026

Brand Name: CGuard Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840

Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98922
Lot/product code:
UDI: 07290120281707; all lots/serial numbers manufactured between 02/03/2025 and 02/23/2026
Recalling firm:
INSPIREMD Inc
View official FDA record (opens in a new tab)